Dose Escalation Study to Investigate the Safety, Tolerability and Pharmacokinetics of ASP2215 in Japanese Patients With Relapsed or Refractory Acute Myeloid Leukemia
- Registration Number
- NCT02181660
- Lead Sponsor
- Astellas Pharma Inc
- Brief Summary
The objectives of this study are to determine the safety and tolerability of ASP2215 as well as the maximum tolerated dose (MTD) based on the onset of dose limiting toxicity (DLT) and/or determine the recommended dose (RD) of ASP2215 for the next phase in subjects with relapsed or treatment-refractory acute myeloid leukemia (AML).
- Detailed Description
This study will be conducted to determine the safety, tolerability, PK, PD, and efficacy of single and repeated oral dosing of ASP2215 once daily in patients with relapsed or refractory AML. After the determination of the MTD and/or RD, an expansion cohort might be set to further investigate the safety and efficacy of ASP2215.
This study will consist of a single-dose period (Cycle 0, 2 days) and a repeated-dose period (Cycle 1 and subsequent cycles, each cycle consisting of 28 days). The enrolled subjects will orally receive their assigned single dose in Cycle 0 (Day -2), followed by a 2-day observation period (dosing day inclusive). In Cycle 1 and subsequent cycles (one cycle is defined as 28 days), the subjects will receive oral ASP2215 once daily repeatedly until one of the discontinuation criteria is met. Another dosing regimen may be considered such as dosing twice daily based on the safety and PK data that will become available.
In this study, the Bayesian-Continual Reassessment Method (hereinafter, Bayesian-CRM) will be used as a reference for dose-escalation procedures, and based on the onset of DLTs, the RD level of the subsequent cohort will be set higher or lower. DLTs will be assessed during Cycle 0 and Cycle 1 (30 days).
ASP2215 may be escalated by one dose level if the subject meets the criteria at the end of each cycle after Cycle 1 and the investigator/sub-investigator judges escalation of ASP2215 is of clinical benefit. Dose reduction of ASP2215 will be considered if study drug-related toxicities are observed in a subject.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 24
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Subject is defined as morphologically documented primary or secondary acute myeloid leukemia (AML) according to the World Health Organization (WHO) criteria (2008) and fulfills one of the following:
- Refractory to prior induction chemotherapy
- Relapsed after achieving remission with prior therapy
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Subject has an Eastern Cooperative Oncology Group (ECOG) performance status of ≤ 2
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Subject's interval from prior treatment to the time of study drug administration is at least 14 days for antineoplastic agents other than ASP2215 (except for hydroxyurea, which is given to control blast cells).
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Subject's interval from prior treatment to the time of study drug (ASP2215) administration is at least 5 half-lives (if the half-life is unknown, 14 days) for other investigational products or drugs used for immunosuppressive therapy posthematopoietic stem cell transplantation (HSCT).
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Subject was diagnosed with acute promyelocytic leukemia (APL).
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Subject has breakpoint cluster region-abelson (BCR-ABL)-positive leukemia (chronic myelogenous leukemia in blast crisis)
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Subject has active malignant tumors other than AML or myelodysplastic syndrome (MDS)
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Subject has persistent non-hematological toxicities of ≥ Grade 2 (CTCAE v4), with symptoms and objective findings, due to prior AML treatment (including chemotherapy, kinase inhibitors, immunotherapy, investigational products, radiation therapy, and surgery)
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Subject has received hematopoietic stem cell transplant (HSCT) and falls under either of the following:
- Is within 2 months of transplant
- Has persistent and clinically significant graft-versus-host disease requiring treatment
- Has persistent non-hematological toxicities of ≥ Grade 2 related to the transplant
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Subject has clinically active central nervous system leukemia
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Subject has disseminated intravascular coagulation (DIC)
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Subject has had major surgery within 28 days prior to the first study drug administration
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Subject has had radiation therapy within 28 days prior to the first study drug administration
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Subject has congestive heart failure of NYHA class 3 or 4, or subject with a past history of congestive heart failure of NYHA class 3 or 4 and in whom echocardiogram or Multiple Gate Acquisition (MUGA) scan performed within 3 months prior to screening or at screening showed a left ventricular ejection fraction (LVEF) of < 45%.
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Subject requires treatment with concomitant drugs that are strong inhibitors or inducers of CYP3A4 or of P-gp with such exceptions of antibiotics, antifungals, and antivirals that are considered absolutely essential for prevention or treatment of infections and for which the physician judged that there are no interchangeable drugs.
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Subject requires treatment with concomitant drugs that target serotonin 5HT1R or 5HT2BR receptors or sigma nonspecific receptors, with the exception of drugs that are considered absolutely essential for treatment of the subject.
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Subject has an active uncontrollable infection
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Subject is known to have human immunodeficiency virus (HIV) infection
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Subject has active hepatitis B or C or other active hepatic disorders
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Dose Escalation Cohort Gilteritinib ASP2215
- Primary Outcome Measures
Name Time Method Safety and Tolerability assessed through adverse events to determine maximum tolerated dose Up to 17 months
- Secondary Outcome Measures
Name Time Method Pharmacokinetics of ASP2215: tmax Cycle 0 Day -2 through Cycle 1 Day 1 and Cycle 1 Day 28 Time to attain Cmax
Pharmacokinetics of ASP2215 in plasma: Rac(AUC) Cycle 1 Day 28 Accumulation ratio calculated using the area under the concentration-time curve
Pharmacokinetics of ASP2215 in plasma: Cmax Cycle 0 Day -2 through Cycle 1 Day 1 and Cycle 1 Day 28 Maximum concentration
Pharmacokinetics of ASP2215 in plasma: C24 Cycle 0 Day -2 through Cycle 1 Day 1 and Cycle 1 Day 28 Concentration at 24 hours
Pharmacokinetics of ASP2215 in plasma: t1/2 Cycle 0 Day -2 through Cycle 1 Day 1 Apparent terminal elimination half-life
Pharmacokinetics of ASP2215 in plasma: Rac(Cmax) Cycle 1 Day 28 Accumulation ratio calculated using the maximum concentration
Pharmacokinetics of ASP2215 in plasma: Rac derived t1/2 Cycle 1 Day 28 t1/2 derived from accumulation index
Pharmacokinetics of ASP2215 in urine: Ae24 Cycle 0 Day -2 through Cycle 1 Day 1 Amount of drug excreted in urine from time 0 to 24 hours
Pharmacokinetics of ASP2215 in urine: Ae48% Cycle 0 Day -2 through Cycle 1 Day 1 Fraction of drug excreted into urine from time 0 to 48 hours as % of dose
Pharmacokinetics of ASP2215 in urine: Aetau Cycle 1 Day 28 Amount of drug excreted in urine during a dosing interval
Pharmacokinetics of ASP2215 in urine: Ae24% Cycle 0 Day -2 through Cycle 1 Day 1 Fraction of drug excreted into urine from time 0 to 24 hours as % of dose
Pharmacokinetics of ASP2215 in urine: CLR Cycle 0 Day -2 through Cycle 1 Day 1 and Cycle 1 Day 28 Renal clearance
Pharmacokinetics of ASP2215 in urine: Aetau % Cycle 1 Day 28 Fraction of drug excreted in urine during a dosing interval
Response Rate Up to 16 months Response Rate includes following parameters; CR rate, composite CR \[CR + CRp + CRi\] rate, overall response rate \[CRc + PR\], duration of response
Pharmacokinetics of ASP2215 in plasma: AUCinf Cycle 0 Day -2 through Cycle 1 Day 1 Area under the concentration-time curve from the time of dosing extrapolated to time infinity
Pharmacokinetics of ASP2215 in plasma: AUC24 Cycle 0 Day -2 through Cycle 1 Day 1 Area under the plasma concentration time curve from time 0 to 24 hours
Pharmacokinetics of ASP2215 in plasma: AUC48 Cycle 0 Day -2 through Cycle 1 Day 1 Area under the plasma concentration time curve from time 0 to 48 hours
Pharmacokinetics of ASP2215 in plasma: Lambda z Cycle 0 Day -2 through Cycle 1 Day 1 Terminal first order elimination rate constant
Pharmacokinetics of ASP2215 in plasma: Vz/F Cycle 0 Day -2 through Cycle 1 Day 1 Apparent volume of distribution during the terminal elimination phase after oral dosing
Pharmacokinetics of ASP2215 in plasma: AUCtau Cycle 1 Day 28 Area under the plasma concentration time curve during a dosing interval
Pharmacokinetics of ASP2215 in plasma: PTR Cycle 1 Day 28 Peak-trough ratio
Pharmacokinetics of ASP2215 in plasma: Ctrough Cycle 1 Day 8, Day 15, Day 22, Day 28 and Day 29 Plasma trough concentration
Pharmacokinetics of ASP2215 in urine: Ae48 Cycle 0 Day -2 through Cycle 1 Day 1 Amount of drug excreted in urine from time 0 to 48 hours
Pharmacokinetics of ASP2215 in plasma: CLF Cycle 0 Day -2 through Cycle 1 Day 1 and Cycle 1 Day 28 Oral clearance
Pharmacokinetics of ASP2215 in plasma: AUClast Cycle 0 Day -2 through Cycle 1 Day 1 Area under the concentration-time curve from the time of dosing to the last measurable concentration
Trial Locations
- Locations (5)
Site JP00001
🇯🇵Gunma, Japan
Site JP00004
🇯🇵Tokyo, Japan
Site JP00005
🇯🇵Tokyo, Japan
Site JP00002
🇯🇵Aichi, Japan
Site JP00003
🇯🇵Fukuoka, Japan